Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121908586
rs121908586
PDGFRA
1.000 0.080 4 54274869 missense variant T/A;C snv
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
Gastrointestinal Stromal Tumors 		0.720 1.000 2 2003 2014
dbSNP: rs121908586
rs121908586
PDGFRA
1.000 0.080 4 54274869 missense variant T/A;C snv
CUI: C0206754
Disease: Neuroendocrine Tumors
Neuroendocrine Tumors 		0.010 < 0.001 1 2007 2007
dbSNP: rs121908586
rs121908586
PDGFRA
1.000 0.080 4 54274869 missense variant T/A;C snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2007 2007
dbSNP: rs121908586
rs121908586
PDGFRA
1.000 0.080 4 54274869 missense variant T/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 < 0.001 1 2007 2007